Evidence map›Paper›PMID 39288015›Full record

ArticleThe Journal of antimicrobial chemotherapy2024

Efficacy and safety of co-trimoxazole in device-related bone and joint infections: a CRIOGO multicentre case-control study.

Raphaël Lecomte, Colin Deschanvres, Amandine Le Bourgeois, Géraldine Bart, Rafaël Mahieu, Gwénaël Le Moal, Séverine Ansart, Nathalie Asseray, Louise Ruffier d'Epenoux, Stéphane Corvec and 2 more

Abstract readMulticenter Study
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Infected total knee arthroplasty: could cotrimoxazole be the answer?European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Raphaël LecomteDepartment of Infectious Diseases, CHU Hôtel-Dieu, Nantes, France.
Colin DeschanvresDepartment of Infectious Diseases, CHU Hôtel-Dieu, Nantes, France.ORCID 0000-0002-1133-5207
Amandine Le BourgeoisDepartment of Hematology, CHU Hôtel-Dieu, Nantes, France.
Géraldine BartDepartment of Rheumatology and Internal Medicine, Percy Military Training Hospital, Paris, France.
Rafaël MahieuDepartment of Infectious Diseases, CHU Angers, Angers, France.
Gwénaël Le MoalDepartment of Infectious Diseases, CHU de Poitiers, Poitiers, France.
Séverine AnsartDepartment of Infectious Diseases, CHU Brest, Brest, France.
Nathalie AsserayDepartment of Infectious Diseases, CHU Hôtel-Dieu, Nantes, France.
Louise Ruffier d'EpenouxDepartment of Bacteriology, CHU Nantes, Nantes, France.
Stéphane CorvecDepartment of Bacteriology, CHU Nantes, Nantes, France.ORCID 0000-0003-3176-8111
David BoutoilleDepartment of Infectious Diseases, CHU Hôtel-Dieu, Nantes, France.ORCID 0000-0001-9722-2029
CRIOGO network

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesCo-trimoxazole could be an alternative antibiotic to treat device-related bone and joint infection (BJI) but there are few published data about its efficacy and safety in this complex scenario to treat infection. The objective was to compare the outcome of patients with device-related BJI treated with an antibiotic regimen including co-trimoxazole versus a regimen without co-trimoxazole.

methodsThis multicentre case-control study included consecutive adult patients diagnosed with device-related BJI. Each patient receiving co-trimoxazole was included in the co-trimoxazole group and was matched with two control patients, with stratification on microbial aetiology and age. The primary outcome was composite and defined by death or treatment failure during the follow-up.

resultsIn this study, 150 patients were included, 50 in the co-trimoxazole group and 100 in the control group. The rate of reaching the primary endpoint was 18% in the co-trimoxazole group (9/50 cases) versus 21% in the control group (21/100) (P = 0.66). Co-trimoxazole use was not associated with an unfavourable outcome in the multivariate analysis (adjusted OR 0.8, 95% CI 0.31-2.06, P = 0.64). Although no significant difference was observed in premature discontinuation of treatment due to an adverse event between both groups (14 versus 12%, P = 0.73), treatment-related adverse events were significantly more frequently reported in patients of the co-trimoxazole group than the control group [34% (17/50) versus 18% (18/100), P = 0.03].

conclusionsCo-trimoxazole appears to be an effective alternative for the treatment of BJI, even when it occurs on a device, but the safety profile requires close monitoring of adverse effects.

Indexed as

Anti-Bacterial AgentsTrimethoprim, Sulfamethoxazole Drug CombinationAdultAgedAged, 80 and overArthritis, InfectiousCase-Control StudiesFemaleHumansMaleMiddle AgedProsthesis-Related InfectionsTreatment OutcomeAnti-Bacterial AgentsTrimethoprim, Sulfamethoxazole Drug Combination

Identifiers

PMID39288015
PMCPMC11637995

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.